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      Small intestinal eosinophils regulate Th17 cells by producing IL-1 receptor antagonist

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          Abstract

          Jang et al. show that eosinophils in the small intestine can suppress Th17 cell differentiation through the secretion of the IL-1 receptor antagonist.

          Abstract

          Eosinophils play proinflammatory roles in helminth infections and allergic diseases. Under steady-state conditions, eosinophils are abundantly found in the small intestinal lamina propria, but their physiological function is largely unexplored. In this study, we found that small intestinal eosinophils down-regulate Th17 cells. Th17 cells in the small intestine were markedly increased in the ΔdblGATA-1 mice lacking eosinophils, and an inverse correlation was observed between the number of eosinophils and that of Th17 cells in the small intestine of wild-type mice. In addition, small intestinal eosinophils suppressed the in vitro differentiation of Th17 cells, as well as IL-17 production by small intestinal CD4 + T cells. Unlike other small intestinal immune cells or circulating eosinophils, we found that small intestinal eosinophils have a unique ability to constitutively secrete high levels of IL-1 receptor antagonist (IL-1Ra), a natural inhibitor of IL-1β. Moreover, small intestinal eosinophils isolated from IL-1Ra−deficient mice failed to suppress Th17 cells. Collectively, our results demonstrate that small intestinal eosinophils play a pivotal role in the maintenance of intestinal homeostasis by regulating Th17 cells via production of IL-1Ra.

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          Most cited references34

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          Regional specialization within the intestinal immune system.

          The intestine represents the largest compartment of the immune system. It is continually exposed to antigens and immunomodulatory agents from the diet and the commensal microbiota, and it is the port of entry for many clinically important pathogens. Intestinal immune processes are also increasingly implicated in controlling disease development elsewhere in the body. In this Review, we detail the anatomical and physiological distinctions that are observed in the small and large intestines, and we suggest how these may account for the diversity in the immune apparatus that is seen throughout the intestine. We describe how the distribution of innate, adaptive and innate-like immune cells varies in different segments of the intestine and discuss the environmental factors that may influence this. Finally, we consider the implications of regional immune specialization for inflammatory disease in the intestine.
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            The IL-1 family: regulators of immunity.

            Over recent years it has become increasingly clear that innate immune responses can shape the adaptive immune response. Among the most potent molecules of the innate immune system are the interleukin-1 (IL-1) family members. These evolutionarily ancient cytokines are made by and act on innate immune cells to influence their survival and function. In addition, they act directly on lymphocytes to reinforce certain adaptive immune responses. This Review provides an overview of both the long-established and more recently characterized members of the IL-1 family. In addition to their effects on immune cells, their involvement in human disease and disease models is discussed.
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              Critical regulation of early Th17 cell differentiation by interleukin-1 signaling.

              T helper (Th) 17 cells have been recently discovered in both mouse and human. Here we show that interleukin-1 (IL-1) signaling on T cells is critically required for the early programming of Th17 cell lineage and Th17 cell-mediated autoimmunity. IL-1 receptor1 expression in T cells, which was induced by IL-6, was necessary for the induction of experimental autoimmune encephalomyelitis and for early Th17 cell differentiation in vivo. Moreover, IL-1 signaling in T cells was required in dendritic cell-mediated Th17 cell differentiation from naive or regulatory precursors and IL-1 synergized with IL-6 and IL-23 to regulate Th17 cell differentiation and maintain cytokine expression in effector Th17 cells. Importantly, IL-1 regulated the expression of the transcription factors IRF4 and RORgammat during Th17 cell differentiation; overexpression of these two factors resulted in IL-1-independent Th17 cell polarization. Our data thus indicate a critical role of IL-1 in Th17 cell differentiation and this pathway may serve as a unique target for Th17 cell-mediated immunopathology.
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                Author and article information

                Journal
                J Exp Med
                J. Exp. Med
                jem
                jem
                The Journal of Experimental Medicine
                The Rockefeller University Press
                0022-1007
                1540-9538
                4 April 2016
                : 213
                : 4
                : 555-567
                Affiliations
                [1 ]Department of Respiratory Medicine, Allergy, and Rheumatic Diseases, Graduate School of Medicine, Osaka University, 565-0871 Suita, Japan
                [2 ]Department of Microbiology and Immunology, Graduate School of Medicine, Osaka University, 565-0871 Suita, Japan
                [3 ]Academy of Immunology and Microbiology, Institute for Basic Science, 790-784 Pohang, Republic of Korea
                [4 ]Division of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology, 790-784 Pohang, Republic of Korea
                [5 ]Department of Life Sciences, Pohang University of Science and Technology, 790-784 Pohang, Republic of Korea
                [6 ]Department of Microbiology, Graduate School of Medicine, Ewha Womans University, 158-710 Seoul, Republic of Korea
                [7 ]Department of Microbiology, School of Medicine, Gachon University, 21936 Incheon, Republic of Korea
                [8 ]WPI Immunology Frontier Research Center, Osaka University, 565-0871 Suita, Japan
                [9 ]MediCity Research Laboratory, University of Turku, 20520 Turku, Finland
                [10 ]Viral Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, 34141 Daejeon, Republic of Korea
                Author notes
                Myoung Ho Jang: jangmh@ 123456ibs.re.kr ; or Bo-Gie Yang: yangbg@ 123456ibs.re.kr
                [*]

                R. Sugawara and E.-J. Lee contributed equally to this paper.

                [**]

                M.H. Jang and B.-G. Yang contributed equally to this paper.

                Article
                20141388
                10.1084/jem.20141388
                4821642
                26951334
                5c8279ba-5b95-4c44-8e67-a9337f4f69bc
                © 2016 Sugawara et al.

                This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

                History
                : 23 July 2014
                : 05 February 2016
                Funding
                Funded by: Institute for Basic Science http://dx.doi.org/10.13039/501100003716
                Award ID: IBS-R005-S1-2015-a00
                Award ID: IBS-R005-D1-2015-a00
                Funded by: National Research Foundation of Korea http://dx.doi.org/10.13039/501100003725
                Award ID: NRF-2015R1A2A2A04003471
                Funded by: Ministry of Education http://dx.doi.org/10.13039/501100002701
                Award ID: R31-10105
                Funded by: Ministry of Education, Culture, Sports, Science and Technology of Japan http://dx.doi.org/10.13039/501100001700
                Award ID: 18790338
                Award ID: 19041044
                Categories
                Research Articles
                Article

                Medicine
                Medicine

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